A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562258



Internal ID16349667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71307417..71359172hg38UCSC Ensembl
Innerchr13:71881549..71933304hg19UCSC Ensembl
Innerchr13:70779550..70831305hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3851756
hg1951756
hg1851756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3240n54
Supporting Variantsnssv813805
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562258
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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